Quantitative image analysis of the extracellular matrix of esophageal squamous cell carcinoma and high grade dysplasia via two-photon microscopy.

Journal: Scientific reports
Published Date:

Abstract

Squamous cell carcinoma (SCC) and high-grade dysplasia (HGD) are two different pathological entities; however, they sometimes share similarities in histological structure depending on the context. Thus, distinguishing between the two may require careful examination by a pathologist and consideration of clinical findings. Unlike previous studies on cancer diagnosis using two-photon microscopy, quantitative analysis or machine learning (ML) algorithms need to be used to determine the subtle structural changes in images and the structural features that are statistically meaningful in cancer development. In this study, we aimed to quantitatively distinguish between SCC and HGD using two-photon microscopy combined with ML. Tissue samples were categorized into two groups: Group 1, primary SCC vs. metachronous HGD (SCC-HGD) and Group 2, primary HGD vs. metachronous HGD (HGD-HGD). We quantitatively analyzed second harmonic generation (SHG) and two-photon fluorescence (TPF) signals from two-photon microscopy imaging of the extracellular matrix (ECM). Gray-level co-occurrence matrix (GLCM) was used to extract the textural features of the tissue images, and support vector machine (SVM), for classification of the tissue images based on their pathologies. The SHG-based classifiers demonstrated 75%, 84.21%, 95%, and 95.65% for Group 1, Group 2, primary SCC vs. primary HGD, and metachronous HGD (Group 1) vs. metachronous HGD (Group 2), respectively. This integrative approach enabled the characterization of different pathological stages and enhances the understanding of the pathogenic factors involved in the progression of esophageal cancer.

Authors

  • Kausalya Neelavara Makkithaya
    Department of Biophysics, Manipal School of Life Sciences, Manipal Academy of Higher Education, Manipal, 576104, India.
  • Wei-Chung Chen
    Division of Gastroenterology, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, 807, Taiwan.
  • Chun-Chieh Wu
    Department of Pathology, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, 807, Taiwan.
  • Ming-Chi Chen
    Institute of Translational Medicine and New Drug Development, Medical University, Taichung, 404328, Taiwan.
  • Wei-Hsun Wang
    Department of Orthopedic Surgery, Changhua Christian Hospital, Changhua 500209, Taiwan.
  • Jackson Rodrigues
    Department of Biophysics, Manipal School of Life Sciences, Manipal Academy of Higher Education, Manipal, Karnataka, India.
  • Ming-Tsang Wu
    Department of Family Medicine, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung, 807, Taiwan.
  • Nirmal Mazumder
    Department of Biophysics, Manipal School of Life Sciences, Manipal Academy of Higher Education, Manipal, 576104, Karnataka, India.
  • I-Chen Wu
    Department of Computer Science, National Yang Ming Chiao Tung University, Hsinchu, Taiwan.
  • Guan-Yu Zhuo
    Institute of Biophotonics, National Yang Ming Chiao Tung University, Taipei, 11221, Taiwan. zhuo0929@nycu.edu.tw.